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Comparison of Laparoscopic Cornuostomy and Wedge Resection for Interstitial Pregnancy

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ClinicalTrials.gov Identifier: NCT03064594
Recruitment Status : Recruiting
First Posted : February 27, 2017
Last Update Posted : May 23, 2018
Sponsor:
Information provided by (Responsible Party):
Sheng-Mou Hsiao, Far Eastern Memorial Hospital

Brief Summary:
This retrospective study is to find out the best way to treat patient with cornual pregnancy in the aspect of further pregnancy outcome.

Condition or disease Intervention/treatment
Cornual Pregnancy Procedure: Cornual pregnancy

Detailed Description:
To find out the best way to treat patient with cornual pregnancy in the aspect of further pregnancy outcome, the investigators compared the outcomes of laparoscopic wedge resection (LWR) and laparoscopic cornuostomy (LC) by the retrospective chart review.

Study Type : Observational
Estimated Enrollment : 40 participants
Observational Model: Case-Control
Time Perspective: Retrospective
Official Title: Comparison of Laparoscopic Cornuostomy and Wedge Resection for Interstitial Pregnancy
Actual Study Start Date : February 9, 2017
Estimated Primary Completion Date : December 31, 2018
Estimated Study Completion Date : December 31, 2018

Group/Cohort Intervention/treatment
cornuostomy
cornuostomy
Procedure: Cornual pregnancy
we will get the information of operative time, blood loss and postoperative pregnancy and delivery rate.

wedge resection
wedge resection



Primary Outcome Measures :
  1. pregnancy rate [ Time Frame: 9 years ]
    pregnancy rate after surgery



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Ages Eligible for Study:   20 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
the cases with cornual pregnancy
Criteria

Inclusion Criteria:

  • All women with cornual pregnancy who were admitted to the Department of Obstetrics and Gynecology of the Far Eastern Memorial Hospital for laparoscopic surgeries between January 2008 and June 2016 were enrolled

Exclusion Criteria:

  • The person who was pregnant at the time of the operation
  • After receiving IVF course of treatment
  • Patients with uterine horns undergoing open surgery

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03064594


Contacts
Contact: Sheng-Mou Hsiao, MD +89667000 ext 1818 smhsiao2@gmail.com

Locations
Taiwan
Department of Obstetrics and Gynecology, Far-Eastern Memorial Hospital Recruiting
New Taipei, Banqiao, Taiwan, 22060
Contact: Sheng-Mou Hsiao, M.D.    +886-2-89667000 ext 1424    smhsiao2@gmail.com   
Sponsors and Collaborators
Far Eastern Memorial Hospital

Responsible Party: Sheng-Mou Hsiao, Chief, Department of Obstetrics & Gynecology, Far Eastern Memorial Hospital
ClinicalTrials.gov Identifier: NCT03064594     History of Changes
Other Study ID Numbers: 105143-E
First Posted: February 27, 2017    Key Record Dates
Last Update Posted: May 23, 2018
Last Verified: April 2018

Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
Pregnancy, Interstitial
Pregnancy, Cornual
Pregnancy, Tubal
Pregnancy, Ectopic
Pregnancy Complications